JP2009201984A - Surgical treatment apparatus - Google Patents

Surgical treatment apparatus Download PDF

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JP2009201984A
JP2009201984A JP2009021676A JP2009021676A JP2009201984A JP 2009201984 A JP2009201984 A JP 2009201984A JP 2009021676 A JP2009021676 A JP 2009021676A JP 2009021676 A JP2009021676 A JP 2009021676A JP 2009201984 A JP2009201984 A JP 2009201984A
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unit
holding member
vibration transmission
treatment apparatus
surgical treatment
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JP5043054B2 (en
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Hideo Sanai
秀男 佐内
Kenichi Kimura
健一 木村
Masashi Yamada
将志 山田
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Olympus Medical Systems Corp
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Olympus Medical Systems Corp
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/0046Surgical instruments, devices or methods, e.g. tourniquets with a releasable handle; with handle and operating part separable
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/00477Coupling
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/320069Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic for ablating tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/320071Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with articulating means for working tip
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/320082Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic for incising tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/320089Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic node location
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B17/320092Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with additional movable means for clamping or cutting tissue, e.g. with a pivoting jaw
    • A61B2017/320094Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with additional movable means for clamping or cutting tissue, e.g. with a pivoting jaw additional movable means performing clamping operation

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  • Health & Medical Sciences (AREA)
  • Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Mechanical Engineering (AREA)
  • Biomedical Technology (AREA)
  • Dentistry (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Surgical Instruments (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a surgical treatment apparatus for treating living tissue, capable of being appropriately operated. <P>SOLUTION: In a second unit 22 of the surgical treatment apparatus, an elastic member 67 is disposed between a second vibration transmitting member 61 and a second holder member 54. The elastic member 67 is deformed according to the relative disposition of the second vibration transmitting member 61 to the second holder member 54 in the axial direction to apply elastic force in the axial direction to the second vibration transmitting member 61. Regulating connection mechanisms 69 and 74 of the surgical treatment apparatus connect a first unit 21 to the second unit 22 to coaxially dispose a first vibration transmitting member 31 of the first unit 21 and the second vibration transmitting member 61 of the second unit 22. The quantity of deformation of the elastic member 67 is regulated by making an end of the first vibration transmitting member 31 and an end of the second vibration transmitting member 61 abut to each other and regulating the relative disposition of a first holder member 39 to the second holder member 54 in the coaxial direction. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、生体組織を処置する外科処置装置に関する。   The present invention relates to a surgical treatment apparatus for treating living tissue.

特許文献1には、外科処置装置としての超音波処置装置が開示されている。超音波処置装置では、ハンドピース組体に外科器具が着脱自在である。ハンドピース組体には、超音波振動を拡大して伝達するホーンが挿通されている。外科器具の筒状のハウジングには、超音波振動を伝達する伝達ロッドが挿通されている。ハウジングの先端部は内径が細く、段差面が形成されており、伝達ロッドにはフランジが形成されており、段差面とフランジとの間には弾性部材が介設されている。ハンドピース組体の先端部と外科器具の基端部とが連結されることにより、ハンドピース組体のホーンの先端部と外科器具の伝達ロッドの基端部とが互いに押圧、連結される。ハンドピースと外科器具の連結方法としては、螺合が採用されており、その他、スナップオン結合、ねじりロックばめが列挙されている。   Patent Document 1 discloses an ultrasonic treatment apparatus as a surgical treatment apparatus. In the ultrasonic treatment apparatus, a surgical instrument is detachable from the handpiece assembly. A horn that magnifies and transmits ultrasonic vibrations is inserted through the handpiece assembly. A transmission rod for transmitting ultrasonic vibration is inserted through the cylindrical housing of the surgical instrument. The front end of the housing has a narrow inner diameter and a stepped surface. The transmission rod has a flange. An elastic member is interposed between the stepped surface and the flange. By connecting the distal end portion of the handpiece assembly and the proximal end portion of the surgical instrument, the distal end portion of the horn of the handpiece assembly and the proximal end portion of the transmission rod of the surgical instrument are pressed and connected to each other. As a method of connecting the handpiece and the surgical instrument, screwing is employed, and other examples include snap-on coupling and torsion lock fit.

欧州特許第893971号明細書European Patent No. 893971

特許文献1のような超音波処置装置では、超音波処置装置が適切に作動されるためには、ホーンの先端部と伝達ロッドの基端部との間に作用する押圧力量を適切な一定の範囲内とする必要がある。しかしながら、特許文献1には、押圧力量を調整するための具体的構成は何ら開示されていない。   In the ultrasonic treatment apparatus such as Patent Document 1, in order for the ultrasonic treatment apparatus to be appropriately operated, the amount of pressing force acting between the distal end portion of the horn and the proximal end portion of the transmission rod is appropriately constant. Must be within range. However, Patent Document 1 does not disclose any specific configuration for adjusting the amount of pressing force.

本発明は、上記課題に着目してなされたもので、その目的とするところは、適切に作動可能な外科処置装置を提供することである。   The present invention has been made paying attention to the above problems, and an object of the present invention is to provide a surgical apparatus that can be appropriately operated.

本発明の第1実施態様では、外科処置装置は、軸方向に延び端部を有し超音波振動を伝達する第1の振動伝達部材、及び、前記第1の振動伝達部材を保持している第1の保持部材、を有する第1のユニットと、軸方向に延び端部を有し超音波振動を伝達する第2の振動伝達部材、前記第2の振動伝達部材の軸方向に移動可能に前記第2の振動伝達部材を保持している第2の保持部材、及び、前記第2の振動伝達部材と前記第2の保持部材との間に設けられ、前記第2の振動伝達部材の軸方向についての前記第2の振動伝達部材と前記第2の保持部材との相対的配置に応じて変形され、前記第2の振動伝達部材に前記第2の振動伝達部材の軸方向への弾性力を付与する弾性部材、を有する第2のユニットと、前記第1のユニットと前記第2のユニットとを互いに連結し、前記第1の振動伝達部材と前記第2の振動伝達部材とを共軸に配置して前記第1の振動伝達部材の端部と前記第2の振動伝達部材の端部とを互いに当接させると共に、共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的配置を一定に調整することにより前記弾性部材の変形量を一定に調整する調整連結機構と、を具備することを特徴とする。   In a first embodiment of the present invention, a surgical treatment apparatus holds a first vibration transmission member that extends in the axial direction and has an end to transmit ultrasonic vibrations, and the first vibration transmission member. A first unit having a first holding member; a second vibration transmission member having an end portion extending in the axial direction and transmitting ultrasonic vibration; and being movable in the axial direction of the second vibration transmission member A second holding member holding the second vibration transmitting member; and a shaft of the second vibration transmitting member provided between the second vibration transmitting member and the second holding member. The second vibration transmission member is deformed according to the relative arrangement of the second vibration transmission member and the second holding member with respect to the direction, and the second vibration transmission member has an elastic force in the axial direction of the second vibration transmission member A second unit having an elastic member for providing the first unit, and the second unit. Are connected to each other, and the first vibration transmission member and the second vibration transmission member are arranged coaxially, so that the end of the first vibration transmission member and the second vibration transmission member The amount of deformation of the elastic member is adjusted to be constant by bringing the end portions into contact with each other and adjusting the relative arrangement of the first holding member and the second holding member in the coaxial direction to be constant. And an adjusting connection mechanism.

本発明の第2実施態様では、外科処置装置は、前記調整連結機構は、カム機構を有し、前記カム機構は、前記第1の保持部材と前記第2の保持部材との内の一方の保持部材に設けられている作動部と、前記第1の保持部材と前記第2の保持部材との内の他方の保持部材に設けられ軸を中心として螺旋状に延びている作動受部と、を有し、前記作動部は前記作動受部に沿って移動され、前記作動部が前記作動受部の連結位置に配置された場合に前記第1のユニットと前記第2のユニットとが互いに連結される、ことを特徴とする。   In a second embodiment of the present invention, in the surgical treatment apparatus, the adjustment coupling mechanism has a cam mechanism, and the cam mechanism is one of the first holding member and the second holding member. An operation portion provided in a holding member; an operation receiving portion provided in the other holding member of the first holding member and the second holding member and extending in a spiral shape around an axis; The operating unit is moved along the operating receiving unit, and the first unit and the second unit are connected to each other when the operating unit is disposed at a connecting position of the operating receiving unit. It is characterized by that.

本発明の第3実施態様では、外科処置装置は、前記調整連結機構は、前記弾性部材の弾性力に抗して共軸方向に前記第1の保持部材と前記第2の保持部材とを相対的に移動させるための操作について、必要な操作力量が一定となるように、操作量に対する共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的移動量を、共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的配置に応じて変化させている、ことを特徴とする。   In a third embodiment of the present invention, in the surgical treatment apparatus, the adjustment connecting mechanism causes the first holding member and the second holding member to move relative to each other in a coaxial direction against the elastic force of the elastic member. As for the operation for moving, the relative movement amount of the first holding member and the second holding member in the coaxial direction with respect to the operation amount is shared so that the required operation force amount is constant. The first holding member and the second holding member in the axial direction are changed according to the relative arrangement of the first holding member and the second holding member.

本発明の第4実施態様では、外科処置装置は、前記カム機構は、前記弾性部材の弾性力に抗して共軸方向に前記第1の保持部材と前記第2の保持部材とを相対的に移動させるための回転操作について、回転操作力量が一定となるように、回転角度に対して圧力角を変化させている、ことを特徴とする。   In a fourth embodiment of the present invention, in the surgical treatment apparatus, the cam mechanism relatively moves the first holding member and the second holding member in the coaxial direction against the elastic force of the elastic member. As for the rotation operation for moving the rotation angle, the pressure angle is changed with respect to the rotation angle so that the amount of rotation operation force is constant.

本発明の第5実施態様では、外科処置装置は、前記調整連結機構は、前記第1のユニットと前記第2のユニットとが連結されたことを告知する告知機構を有する、ことを特徴とする。   In a fifth embodiment of the present invention, the surgical treatment apparatus is characterized in that the adjustment coupling mechanism has a notification mechanism for notifying that the first unit and the second unit are coupled. .

本発明の第6実施態様では、外科処置装置は、前記カム機構は、前記作動受部において連結位置の手前で前記作動受部に交差する方向に突没している凹凸形状を有する、ことを特徴とする。   In a sixth embodiment of the present invention, in the surgical treatment apparatus, the cam mechanism has an uneven shape that protrudes and projects in a direction intersecting the operation receiving portion before the connection position in the operation receiving portion. Features.

本発明の第7実施態様では、外科処置装置は、前記調整連結機構は、前記第1のユニットと前記第2のユニットとを共軸を中心とする複数の相対的回転配置で連結可能である、ことを特徴とする。   In a seventh embodiment of the present invention, in the surgical treatment apparatus, the adjustment connecting mechanism can connect the first unit and the second unit in a plurality of relative rotational arrangements around a coaxial axis. It is characterized by that.

本発明の第8実施態様では、外科処置装置は、前記カム機構は、周方向について互いに異なる位置に配置されている第1及び第2の連結位置を有する、ことを特徴とする。   In an eighth embodiment of the present invention, the surgical treatment apparatus is characterized in that the cam mechanism has first and second coupling positions arranged at positions different from each other in the circumferential direction.

本発明の第9実施態様では、外科処置装置は、前記第2の振動伝達部材は、前記第2の振動伝達部材において軸方向の一端側に形成されている太外径部と、前記第2の振動伝達部材において軸方向の他端側に形成され前記太外径部よりも外径の小さな細外径部と、前記第2の振動伝達部材において前記太外径部と前記細外径部との間に形成され軸方向の一端側から他端側へと外径の減少するテーパ部と、前記テーパ部あるいは前記細外径部に設けられ径方向に突出している押圧部と、を有し、前記弾性部材は、軸方向について前記押圧部と前記第2の保持部材との間に設けられている、ことを特徴とする。   In a ninth embodiment of the present invention, in the surgical treatment apparatus, the second vibration transmission member includes a thick outer diameter portion formed on one end side in the axial direction of the second vibration transmission member, and the second A thin outer diameter portion that is formed on the other end side in the axial direction of the vibration transmission member and has a smaller outer diameter than the thick outer diameter portion, and the thick outer diameter portion and the thin outer diameter portion in the second vibration transmission member. And a taper portion having an outer diameter decreasing from one end side to the other end side in the axial direction, and a pressing portion provided in the taper portion or the thin outer diameter portion and projecting in the radial direction. And the said elastic member is provided between the said press part and the said 2nd holding member about the axial direction, It is characterized by the above-mentioned.

本発明の第1実施態様の外科処置装置では、第1のユニットと第2のユニットとの連結に際して、弾性部材の変形量を一定に調整することで、弾性部材から第2の振動伝達部材に付与される弾性力量を一定に調整し、第1の振動伝達部材と第2の振動伝達部材との間に作用する押圧力量を一定に調整している。このため、第1及び第2の振動伝達部材を適切に作動させることが可能となっている。   In the surgical treatment apparatus according to the first embodiment of the present invention, when the first unit and the second unit are connected, the deformation amount of the elastic member is adjusted to be constant, so that the elastic member changes to the second vibration transmitting member. The amount of elastic force applied is adjusted to be constant, and the amount of pressing force acting between the first vibration transmission member and the second vibration transmission member is adjusted to be constant. For this reason, it is possible to operate the first and second vibration transmitting members appropriately.

本発明の第2実施態様の外科処置装置では、共軸を中心として第1の保持部材と第2の保持部材とを相対的に回転させ、作動部を作動受部に沿って移動させて連結位置に配置することにより、共軸方向について第1の保持部材と第2の保持部材との相対的配置が一定に調整され、弾性部材の変形量が一定に調整される。   In the surgical treatment apparatus according to the second embodiment of the present invention, the first holding member and the second holding member are relatively rotated around the coaxial axis, and the operating portion is moved along the operating receiving portion to be connected. By arranging at the position, the relative arrangement of the first holding member and the second holding member in the coaxial direction is adjusted to be constant, and the deformation amount of the elastic member is adjusted to be constant.

本発明の第3実施態様の外科処置装置では、第1の保持部材と第2の保持部材との連結において、弾性部材の変形量にかかわらず操作力量が一定となるようにしており、連結操作を円滑に行うことが可能となっている。   In the surgical treatment apparatus according to the third embodiment of the present invention, the connection force between the first holding member and the second holding member is such that the amount of operation force is constant regardless of the amount of deformation of the elastic member. Can be performed smoothly.

本発明の第4実施態様の外科処置装置では、カム機構において回転角度に対して圧力角を変化させることにより、弾性部材の変形量にかかわらず回転操作力量が一定となるようにしている。   In the surgical treatment apparatus according to the fourth embodiment of the present invention, the amount of rotational operation force is made constant regardless of the amount of deformation of the elastic member by changing the pressure angle with respect to the rotational angle in the cam mechanism.

本発明の第5実施態様の外科処置装置では、第1のユニットと第2のユニットとが連結されたことを告知するようにしており、第1のユニットと第2のユニットとの連結を認識することが可能となっている。   In the surgical treatment apparatus according to the fifth embodiment of the present invention, the fact that the first unit and the second unit are connected is notified, and the connection between the first unit and the second unit is recognized. It is possible to do.

本発明の第6実施態様の外科処置装置では、作動部が連結位置の手前の凹凸形状を通過することによりクリック感が生じ、このクリック感によって第1のユニットと第2のユニットとの連結を告知するようにしている。   In the surgical treatment apparatus according to the sixth embodiment of the present invention, a click feeling is generated when the operating part passes through the uneven shape in front of the connection position, and the connection between the first unit and the second unit is caused by this click feeling. I am trying to announce.

本発明の第7実施態様の外科処置装置では、第1のユニットと第2のユニットとを共軸を中心とする複数の相対的回転配置の内の所望の相対的回転配置で連結することができ、外科処置装置を当座の処置に適した形態とすることが可能となっている。   In the surgical treatment apparatus according to the seventh embodiment of the present invention, the first unit and the second unit may be coupled in a desired relative rotational arrangement out of a plurality of relative rotational arrangements around the coaxial axis. The surgical apparatus can be configured to be suitable for the current procedure.

本発明の第8実施態様の外科処置装置では、周方向について互いに異なる位置に配置されている第1及び第2の連結位置に作動部を配置可能とすることにより、第1のユニットと第2のユニットとを共軸を中心とする複数の相対的回転配置で連結可能としている。   In the surgical treatment apparatus according to the eighth embodiment of the present invention, the operating unit can be disposed at the first and second coupling positions that are disposed at different positions in the circumferential direction, whereby the first unit and the second unit are arranged. These units can be connected in a plurality of relative rotational arrangements around a coaxial axis.

本発明の第9実施態様の外科処置装置では、第2の振動伝達部材において太外径部よりも細径のテーパ部及び細外径部を形成し、径方向に突出している押圧部をテーパ部あるいは細外径部に設けているため、第2のユニットが太径化することが回避され、外科処置装置の操作性の低下が防止されている。   In the surgical treatment apparatus according to the ninth embodiment of the present invention, the second vibration transmission member is formed with a tapered portion and a thin outer diameter portion that are thinner than the thick outer diameter portion, and the pressing portion protruding in the radial direction is tapered. Therefore, the second unit is prevented from becoming thicker and the operability of the surgical treatment apparatus is prevented from being lowered.

本発明の一実施形態の外科処置具を示す側面図。The side view which shows the surgical treatment tool of one Embodiment of this invention. 本発明の一実施形態の外科処置具を示す縦断面図。The longitudinal cross-sectional view which shows the surgical treatment tool of one Embodiment of this invention. 本発明の一実施形態のカム枠を示す縦断面図。The longitudinal cross-sectional view which shows the cam frame of one Embodiment of this invention. 本発明の一実施形態のカム枠を示す展開図。The expanded view which shows the cam frame of one Embodiment of this invention. 本発明の一実施形態の弾性部材の潰れ量と押圧力量との関係のグラフを示す図。The figure which shows the graph of the relationship between the crushing amount of the elastic member of one Embodiment of this invention, and pressing force amount. 本発明の一実施形態のカム機構の回転角度と圧力角との関係のグラフを示す図。The figure which shows the graph of the relationship between the rotation angle of the cam mechanism of one Embodiment of this invention, and a pressure angle. 本発明の一実施形態の第1変形例の外科処置具を示す部分縦断面側面図。The fragmentary longitudinal cross-section side view which shows the surgical treatment tool of the 1st modification of one Embodiment of this invention. 本発明の一実施形態の第2変形例の外科処置具を示す側面図。The side view which shows the surgical treatment tool of the 2nd modification of one Embodiment of this invention.

以下、本発明の一実施形態を図面を参照して説明する。   Hereinafter, an embodiment of the present invention will be described with reference to the drawings.

図1乃至図5Bは、本発明の一実施形態を示す。   1 to 5B show an embodiment of the present invention.

本実施形態の外科処置装置としての外科処置具は、開腹手術用の超音波出力併用型高周波処置具である。   The surgical treatment tool as the surgical treatment apparatus of this embodiment is an ultrasonic output combined high-frequency treatment tool for laparotomy.

図1乃至図2を参照して、外科処置具の概略構成を説明する。   A schematic configuration of the surgical instrument will be described with reference to FIGS. 1 and 2.

外科処置具は、操作者に保持、操作される第1のユニットとしてのハンドピース21を有する。ハンドピース21は軸方向に延びている。ハンドピース21の基端部から電気ケーブル23が延出されており、電気ケーブル23は装置本体へと接続される。   The surgical instrument has a handpiece 21 as a first unit held and operated by an operator. The handpiece 21 extends in the axial direction. An electric cable 23 extends from the proximal end portion of the handpiece 21, and the electric cable 23 is connected to the apparatus main body.

ハンドピース21には振動子24が収容されており、振動子24はハンドピース21の軸方向に延びている。振動子24の基端部には超音波振動を発生する圧電素子部26が配設されており、振動子24の先端側には超音波振動を拡大して伝達する第1の振動伝達部材としてのホーン31が配設されている。ここで、圧電素子部26には超音波ケーブル33の先端部が接続されており、超音波ケーブル33は電気ケーブル23へと導入されている。装置本体から超音波ケーブル33を介して圧電素子部26に駆動電流が供給されることにより、圧電素子部26において電気的振動が機械的振動に変換され、振動子24が超音波振動される。ここで、振動子24の軸方向長さは超音波振動の1波長の長さであり、圧電素子部26の軸方向長さは超音波振動の1/4波長の長さであり、ホーン31の軸方向長さは超音波振動の3/4波長の長さである。そして、ホーン31の基端は超音波振動の節位置となり、フランジ状の固定部34が形成されている。ホーン31の先端は超音波振動の腹位置となる。一方、圧電素子部26には、高周波ケーブル38の先端部が接続されている。高周波ケーブル38は、電気ケーブル23へと導入されている。装置本体から高周波ケーブル38を介して圧電素子部26に高周波電流が供給されることにより、振動子24に高周波電流が通電される。   A vibrator 24 is accommodated in the handpiece 21, and the vibrator 24 extends in the axial direction of the handpiece 21. A piezoelectric element portion 26 that generates ultrasonic vibration is disposed at the proximal end portion of the vibrator 24, and a first vibration transmission member that expands and transmits the ultrasonic vibration to the distal end side of the vibrator 24. The horn 31 is provided. Here, the tip of an ultrasonic cable 33 is connected to the piezoelectric element portion 26, and the ultrasonic cable 33 is introduced into the electric cable 23. When a drive current is supplied from the apparatus main body to the piezoelectric element portion 26 via the ultrasonic cable 33, electrical vibration is converted into mechanical vibration in the piezoelectric element portion 26, and the vibrator 24 is ultrasonically vibrated. Here, the axial length of the vibrator 24 is the length of one wavelength of ultrasonic vibration, the axial length of the piezoelectric element portion 26 is the length of a quarter wavelength of ultrasonic vibration, and the horn 31. The axial length of is the length of 3/4 wavelength of ultrasonic vibration. And the base end of the horn 31 becomes a node position of ultrasonic vibration, and a flange-shaped fixing portion 34 is formed. The tip of the horn 31 is the antinode position of ultrasonic vibration. On the other hand, the distal end portion of the high-frequency cable 38 is connected to the piezoelectric element portion 26. The high frequency cable 38 is introduced into the electric cable 23. By supplying a high-frequency current from the apparatus main body to the piezoelectric element portion 26 via the high-frequency cable 38, the high-frequency current is passed through the vibrator 24.

振動子24は、第1の保持部材としての内側ハウジング39に収容されている。内側ハウジング39は、軸方向に延び、基端側内筒41と先端側内筒42とによって形成されている。基端側内筒41には圧電素子部26が収容されており、先端側内筒42にはホーン31が収容されている。基端側内筒41の先端側内周面には突出部43が周方向に延設されている。基端側内筒41の先端部には先端側内筒42の基端部が内挿され、螺着されている。基端側内筒41に先端側内筒42を捻じ込むことにより、基端側内筒41の突出部43と先端側内筒42の基端面とによって振動子24の固定部34が挟持されて、固定されている。なお、固定部34の先端面と先端側内筒42の基端面との間には、振動子24の固定位置を軸方向について調整するための環状の固定用スペーサ44が介設されている。   The vibrator 24 is accommodated in an inner housing 39 as a first holding member. The inner housing 39 extends in the axial direction and is formed by a proximal end inner cylinder 41 and a distal end side inner cylinder 42. The proximal end inner cylinder 41 accommodates the piezoelectric element portion 26, and the distal end inner cylinder 42 accommodates the horn 31. A protrusion 43 extends in the circumferential direction on the inner peripheral surface of the distal end side inner cylinder 41. The proximal end portion of the distal end side inner cylinder 42 is inserted into the distal end portion of the proximal end side inner cylinder 41 and screwed. By screwing the distal end side inner cylinder 42 into the proximal end side inner cylinder 41, the fixing portion 34 of the vibrator 24 is sandwiched between the protruding portion 43 of the proximal end side inner cylinder 41 and the proximal end surface of the distal end side inner cylinder 42. It has been fixed. An annular fixing spacer 44 for adjusting the fixing position of the vibrator 24 in the axial direction is interposed between the distal end surface of the fixing portion 34 and the proximal end surface of the distal end inner cylinder 42.

内側ハウジング39は、外側ハウジング47に収容されている。外側ハウジング47には、ハンドスイッチ部49が配設されている。ハンドスイッチ部49には、切開出力スイッチ52a、凝固出力スイッチ52b、同時出力スイッチ52cが配設されている。ハンドスイッチ部49のスイッチ本体51からスイッチケーブル53が延出されており、スイッチケーブル53は、電気ケーブル23へと導入されている。切開出力スイッチ52aを押下操作することにより、装置本体から圧電素子部26に高周波切開処置用の切開電流が出力され、外科処置具が切開出力モードで駆動される。凝固出力スイッチ52bを押下操作することにより、高周波凝固処置用の凝固電流が出力され、外科処置具が凝固出力モードで駆動される。同時出力スイッチ52cを押下操作することにより、高周波処置用の高周波電流と超音波処置用の駆動電流とが同時出力され、外科処置具が同時出力モードで駆動される。   The inner housing 39 is accommodated in the outer housing 47. A hand switch portion 49 is disposed in the outer housing 47. The hand switch unit 49 is provided with an incision output switch 52a, a coagulation output switch 52b, and a simultaneous output switch 52c. A switch cable 53 extends from the switch body 51 of the hand switch unit 49, and the switch cable 53 is introduced into the electric cable 23. By depressing the incision output switch 52a, an incision current for high frequency incision treatment is output from the apparatus main body to the piezoelectric element portion 26, and the surgical instrument is driven in the incision output mode. By depressing the coagulation output switch 52b, a coagulation current for high-frequency coagulation treatment is output, and the surgical instrument is driven in the coagulation output mode. By depressing the simultaneous output switch 52c, a high-frequency current for high-frequency treatment and a drive current for ultrasonic treatment are simultaneously output, and the surgical instrument is driven in the simultaneous output mode.

外科処置具は、生体組織を処置するための第2のユニットとしてのシースユニット22を有する。シースユニット22では、第2の保持部材としての筒状のシース組体54に、第2の振動伝達部材としてのプローブ61が挿通されている。   The surgical instrument has a sheath unit 22 as a second unit for treating living tissue. In the sheath unit 22, a probe 61 as a second vibration transmission member is inserted through a cylindrical sheath assembly 54 as a second holding member.

シース組体54は、先端側シース55と基端側シース56とによって形成されている。先端側シース55では、先端側から基端側へと、細内径部57、中内径部58、太内径部59が順に形成されている。先端側シース55の太内径部59には、基端側シース56の先端部が内挿され、螺着されている。基端側シース56の軸方向中間部には、ハンドピース21に対してシースユニット22を回転操作するための回転ダイヤル60が形成されている。   The sheath assembly 54 is formed by a distal end side sheath 55 and a proximal end side sheath 56. In the distal end side sheath 55, a small inner diameter portion 57, a medium inner diameter portion 58, and a large inner diameter portion 59 are formed in this order from the distal end side to the proximal end side. The distal end portion of the proximal end side sheath 56 is inserted and screwed into the large inner diameter portion 59 of the distal end side sheath 55. A rotation dial 60 for rotating the sheath unit 22 with respect to the handpiece 21 is formed at an axially intermediate portion of the proximal end side sheath 56.

一方、プローブ61では、先端側から基端側へと、処置部62、細外径部63、テーパ部64、太外径部66が順に形成されている。処置部62は、生体組織を処置するためのものであり、非回転対称なフック形状を有する。テーパ部64では、先端側から基端側へと外径が増大しており、テーパ部64にはフランジ状の押圧部65が形成されている。ここで、プローブ61の軸方向長さは超音波振動の1/2波長の長さとなっており、プローブ61の先端及び基端は超音波振動の腹位置となっており、押圧部65は超音波振動の節位置となっている。なお、プローブ61の押圧部65の外径は、太外径部66の外径以下となっている。   On the other hand, in the probe 61, a treatment portion 62, a thin outer diameter portion 63, a taper portion 64, and a thick outer diameter portion 66 are formed in this order from the distal end side to the proximal end side. The treatment section 62 is for treating a living tissue and has a non-rotationally symmetric hook shape. The tapered portion 64 has an outer diameter that increases from the distal end side to the proximal end side, and a flange-shaped pressing portion 65 is formed on the tapered portion 64. Here, the length of the probe 61 in the axial direction is ½ wavelength of the ultrasonic vibration, the tip and the base end of the probe 61 are the antinode positions of the ultrasonic vibration, and the pressing portion 65 is super It is the node position of sonic vibration. Note that the outer diameter of the pressing portion 65 of the probe 61 is equal to or smaller than the outer diameter of the thick outer diameter portion 66.

シースユニット22の先端側シース55の中内径部58には、プローブ61の押圧部65が軸方向に摺動自在かつプローブ61の中心軸を中心として回転不能に内挿されている。即ち、シース組体54に対してプローブ61は軸方向に移動自在かつプローブ61の中心軸を中心として回転不能である。先端側シース55の細内径部57と中内径部58との間の段差面によって、支持面70が形成されている。先端側シース55の支持面70と、プローブ61の押圧部65の先端面との間には、先端側に環状の弾性部材67、基端側に環状の押圧用スペーサ68が配設されている。押圧用スペーサ68は、弾性部材67の潰れ量を調整するためのものである。プローブ61の押圧部65の基端面は、先端側シース55の太内径部59に螺着されている基端側シース56の先端面によって支持されている。即ち、シース組体54の先端側シース55の支持面70と基端側シース56の先端面とによって、シース組体54に対してプローブ61が軸方向に移動自在となるように、弾性部材67、押圧用スペーサ68、プローブ61の押圧部65が軸方向について挟持されている。   A pressing portion 65 of the probe 61 is inserted into the inner diameter portion 58 of the distal end side sheath 55 of the sheath unit 22 so as to be slidable in the axial direction and not rotatable about the central axis of the probe 61. That is, the probe 61 is movable in the axial direction with respect to the sheath assembly 54 and is not rotatable about the central axis of the probe 61. A support surface 70 is formed by a step surface between the small inner diameter portion 57 and the inner inner diameter portion 58 of the distal sheath 55. Between the support surface 70 of the distal sheath 55 and the distal surface of the pressing portion 65 of the probe 61, an annular elastic member 67 is disposed on the distal end side, and an annular pressing spacer 68 is disposed on the proximal end side. . The pressing spacer 68 is for adjusting the crushing amount of the elastic member 67. The proximal end surface of the pressing portion 65 of the probe 61 is supported by the distal end surface of the proximal end side sheath 56 that is screwed to the large inner diameter portion 59 of the distal end side sheath 55. In other words, the elastic member 67 is configured such that the probe 61 is movable in the axial direction with respect to the sheath assembly 54 by the support surface 70 of the distal sheath 55 and the distal surface of the proximal sheath 56 of the sheath assembly 54. The pressing spacer 68 and the pressing portion 65 of the probe 61 are sandwiched in the axial direction.

図2乃至図4を参照して、シースユニット22とハンドピース21とを互いに着脱自在に連結するためのカム機構について説明する。ここで、シースユニット22とハンドピース21とは互いに共軸に連結され、以下では、共軸の周方向一方向きを連結方向、他方向きを分離方向と称する。   A cam mechanism for detachably connecting the sheath unit 22 and the handpiece 21 to each other will be described with reference to FIGS. Here, the sheath unit 22 and the handpiece 21 are connected to each other coaxially, and hereinafter, one direction in the circumferential direction of the coaxial is referred to as a connecting direction and the other direction is referred to as a separating direction.

シースユニット22では、基端側シース56の基端部に、作動部としてのカムピン69が径方向外向きに突設されている。一方、ハンドピース21では、内側ハウジング39の先端側内筒42の先端部に、連結筒71の基端部が共軸に連結されている。連結筒71の先端側には、カム枠72が内挿、固定されている。カム枠72の先端側の内周面には、径方向内向きに凸のカム受部73が形成されている。カム受部73の側面の内、全体として分離方向側かつ基端向きに配置されている側面により、作動受部としてのカム面74が形成されている。カム面74は、先端側から基端側へと、導入面75、作動面76、連結面77をなしている。導入面75は軸方向に延びており、作動面76は全体として分離方向向きかつ基端向きであってカム枠72の中心軸を中心として螺旋状に延びており、連結面77は基端向きであって周方向に延びている。また、連結面77の分離方向端部には基端向きに突出している連結凸面78が形成されており、連結面77の連結方向端部には基端向きに突出している回転凸面79が形成されている。連結凸面78と回転凸面79との間には、カムピン69が係合される連結位置としての係合凹面80が形成されている。そして、4つのカム受部73が周方向に等間隔に配置されている。カム受部73の側面の内、全体として連結方向側かつ先端向きに配置されている側面については、当該カム受部73の連結方向側に隣り合うカム受部73のカム面74に沿うカムピン69の移動を妨げないような形状をなしており、隣り合うカム受部73間には導入溝部82が形成されている。なお、導入溝部82の両側面の先端部には、先端側に向かって周方向に広がり、カムピン69をガイドする一対のガイド面83が形成されている。   In the sheath unit 22, a cam pin 69 serving as an operating portion projects from the proximal end portion of the proximal end side sheath 56 outward in the radial direction. On the other hand, in the handpiece 21, the proximal end portion of the connecting tube 71 is connected to the distal end portion of the distal end side inner tube 42 of the inner housing 39 coaxially. A cam frame 72 is inserted and fixed on the distal end side of the connecting cylinder 71. A cam receiving portion 73 that protrudes inward in the radial direction is formed on the inner peripheral surface on the distal end side of the cam frame 72. Of the side surfaces of the cam receiving portion 73, a cam surface 74 as an operation receiving portion is formed by a side surface that is disposed in the separation direction side and toward the proximal end as a whole. The cam surface 74 forms an introduction surface 75, an operation surface 76, and a connection surface 77 from the distal end side to the proximal end side. The introduction surface 75 extends in the axial direction, the operating surface 76 is generally oriented in the separating direction and toward the proximal end, and extends spirally around the central axis of the cam frame 72, and the connecting surface 77 is directed toward the proximal end. However, it extends in the circumferential direction. Further, a connecting convex surface 78 protruding toward the base end is formed at the end portion in the separation direction of the connecting surface 77, and a rotating convex surface 79 protruding toward the base end is formed at the end portion of the connecting surface 77 in the connecting direction. Has been. An engagement concave surface 80 is formed between the connection convex surface 78 and the rotation convex surface 79 as a connection position where the cam pin 69 is engaged. Four cam receiving portions 73 are arranged at equal intervals in the circumferential direction. Among the side surfaces of the cam receiving portion 73, the cam pins 69 extending along the cam surface 74 of the cam receiving portion 73 adjacent to the connecting direction side of the cam receiving portion 73 as a whole are arranged in the connecting direction side and toward the distal end. The introduction groove portion 82 is formed between the adjacent cam receiving portions 73. It should be noted that a pair of guide surfaces 83 that extend in the circumferential direction toward the distal end side and guide the cam pins 69 are formed at the distal end portions on both side surfaces of the introduction groove portion 82.

ハンドピース21のカム枠72の導入溝部82にシースユニット22のカムピン69を位置合わせし、ハンドピース21の先端部にシースユニット22の基端部を軸方向に内挿することにより、カムピン69はカム枠72の導入溝部82に沿って軸方向に移動される。ここで、シースユニット22に保持されているプローブ61は、ハンドピース21に固定されているホーン31に共軸に配置され、プローブ61の基端面がホーン31の先端面に当接される。シースユニット22をハンドピース21に対して連結方向に回転操作することにより、カムピン69がカム面74の作動面76に沿って移動していき、シースユニット22のシース組体54がハンドピース21に対して基端向きに移動される。ここで、シースユニット22のプローブ61の基端面はハンドピース21のホーン31の先端面に当接されているため、プローブ61はホーン31に対して基端向きに移動不能である。従って、シースユニット22において、プローブ61に対してシース組体54が基端側へと移動されることになり、プローブ61とシース組体54との間に介設されている弾性部材67が軸方向に潰される。弾性部材67は軸方向に潰されることにより、シース組体54に先端向きの押圧力を付与すると共に、プローブ61に基端向きの押圧力を付与する。シース組体54への先端向きの押圧力により、シース組体54のカムピン69は先端側に配置されているカム面74に押圧される。一方、プローブ61への基端向きの押圧力により、プローブ61の基端面とホーン31の先端面との間に押圧力が作用される。さらに、シースユニット22をハンドピース21に対して連結方向に回転操作することにより、カムピン69がカム面74の連結凸面78を乗り越えて係合凹面80へと係合され、シースユニット22とハンドピース21とが連結される。カムピン69がカム面74の連結凸面78を乗り越えて係合凹面80に係合される際に、クリック音等のクリック感が生じるため、シースユニット22とハンドピース21とが連結されたことを認識することが可能である。シースユニット22とハンドピース21とを分離する場合には、ハンドピース21に対してシースユニット22を分離方向に回転操作する。   By positioning the cam pin 69 of the sheath unit 22 in the introduction groove portion 82 of the cam frame 72 of the handpiece 21 and inserting the proximal end portion of the sheath unit 22 into the distal end portion of the handpiece 21 in the axial direction, the cam pin 69 is It is moved in the axial direction along the introduction groove 82 of the cam frame 72. Here, the probe 61 held by the sheath unit 22 is disposed coaxially with the horn 31 fixed to the handpiece 21, and the proximal end surface of the probe 61 is brought into contact with the distal end surface of the horn 31. By rotating the sheath unit 22 in the connecting direction with respect to the handpiece 21, the cam pin 69 moves along the operating surface 76 of the cam surface 74, and the sheath assembly 54 of the sheath unit 22 is moved to the handpiece 21. On the other hand, it is moved toward the proximal end. Here, since the proximal end surface of the probe 61 of the sheath unit 22 is in contact with the distal end surface of the horn 31 of the handpiece 21, the probe 61 cannot move toward the proximal end with respect to the horn 31. Accordingly, in the sheath unit 22, the sheath assembly 54 is moved to the proximal end side with respect to the probe 61, and the elastic member 67 interposed between the probe 61 and the sheath assembly 54 is pivoted. Crushed in the direction. The elastic member 67 is crushed in the axial direction, thereby applying a pressing force toward the distal end to the sheath assembly 54 and applying a pressing force toward the proximal end to the probe 61. The cam pin 69 of the sheath assembly 54 is pressed against the cam surface 74 disposed on the distal end side by the pressing force toward the distal end of the sheath assembly 54. On the other hand, a pressing force acts on the probe 61 between the proximal end surface of the probe 61 and the distal end surface of the horn 31 due to the pressing force toward the proximal end. Further, by rotating the sheath unit 22 in the connecting direction with respect to the handpiece 21, the cam pin 69 gets over the connecting convex surface 78 of the cam surface 74 and is engaged with the engaging concave surface 80, and the sheath unit 22 and the handpiece are engaged. 21 is connected. When the cam pin 69 gets over the connecting convex surface 78 of the cam surface 74 and is engaged with the engaging concave surface 80, a click feeling such as a clicking sound is generated, and it is recognized that the sheath unit 22 and the handpiece 21 are connected. Is possible. When the sheath unit 22 and the handpiece 21 are separated, the sheath unit 22 is rotated with respect to the handpiece 21 in the separation direction.

ここで、プローブ61の基端面とホーン31の先端面との間に作用する押圧力量は弾性部材67からプローブ61に付与される押圧力量に相当し、弾性部材67の押圧力量は弾性部材67の潰れ量によって定まり、弾性部材67の潰れ量はプローブ61に対するシース組体54の軸方向の相対位置によって定まる。さらに、プローブ61に対するシース組体54の軸方向の相対位置はホーン31に対するシース組体54の軸方向の相対位置によって定まり、ハンドピース21において、ホーン31、内側ハウジング39、連結筒71は一体的に固定されているため、ホーン31に対するシース組体54の軸方向の相対位置は連結筒71に対するシース組体54の軸方向の相対位置によって定まる。即ち、プローブ61の基端面とホーン31の先端面との間に作用する押圧力量は、連結筒71に対するシース組体54の軸方向の相対位置によって定まることになる。ハンドピース21にシースユニット22が連結されている場合について、連結筒71に対するシース組体54の軸方向の相対位置は、カム面74の連結面77の軸方向位置、即ち、カム面74の係合凹面80の底面の軸方向位置を適宜設定することにより、非常に正確に定めることが可能である。従って、プローブ61の基端面とホーン31の先端面との間に作用する押圧力量を非常に正確に定めることが可能である。   Here, the amount of pressing force acting between the base end surface of the probe 61 and the tip end surface of the horn 31 corresponds to the amount of pressing force applied from the elastic member 67 to the probe 61, and the amount of pressing force of the elastic member 67 is that of the elastic member 67. The amount of collapse of the elastic member 67 is determined by the relative position in the axial direction of the sheath assembly 54 with respect to the probe 61. Further, the relative position in the axial direction of the sheath assembly 54 with respect to the probe 61 is determined by the relative position in the axial direction of the sheath assembly 54 with respect to the horn 31, and in the handpiece 21, the horn 31, the inner housing 39, and the connecting cylinder 71 are integrated. Therefore, the relative position in the axial direction of the sheath assembly 54 with respect to the horn 31 is determined by the relative position in the axial direction of the sheath assembly 54 with respect to the connecting tube 71. That is, the amount of pressing force acting between the proximal end surface of the probe 61 and the distal end surface of the horn 31 is determined by the relative position in the axial direction of the sheath assembly 54 with respect to the connecting tube 71. In the case where the sheath unit 22 is coupled to the handpiece 21, the relative position in the axial direction of the sheath assembly 54 with respect to the coupling cylinder 71 is the axial position of the coupling surface 77 of the cam surface 74, that is, the engagement of the cam surface 74. By setting the axial position of the bottom surface of the concavity 80 as appropriate, it can be determined very accurately. Therefore, the amount of pressing force acting between the base end surface of the probe 61 and the front end surface of the horn 31 can be determined very accurately.

また、弾性部材67の押圧力量に抗して、シースユニット22をハンドピース21に対して連結方向に回転操作するのに必要な回転操作力量は一定となっている。即ち、図5Aに示されるように、弾性部材67の押圧力量Pは弾性部材67の潰れ量xの増大に対して増大する。連結筒71に対するシース組体54の軸方向の移動量δlに弾性部材67の押圧力量Pを乗じた値が、カム機構の回転角度量δθに回転操作力量Pθを乗じた値に対応することになる。即ち、P(x)*δl∝Pθ*δθである。ここで、カム機構の回転角度θに対してカム面74の作動面76の圧力角αが一定の場合には、カム機構の回転角度量δθに対するシース組体54の軸方向の移動量δl、即ち、δl/δθは一定となる。この場合、カム機構の回転角度θの増大により、弾性部材67の潰れ量xが増大され、押圧力量P(x)が増大されていくにつれて、必要な回転操作力量Pθ∝P(x)*(δl/δθ)が増大されることになる。これに対して、本実施形態では、図5Bに示されるように、カム機構の回転角度θの増大に対してカム面74の作動面76の圧力角αを適宜増大させ、カム機構の回転角度量δθに対するシース組体54の軸方向の移動量δl、即ち、δl/δθを適宜減少させることで、回転操作力量Pθ∝P(x)*(δl/δθ)を一定としている。 Further, the amount of rotational operation force required to rotate the sheath unit 22 in the connecting direction relative to the handpiece 21 against the amount of pressing force of the elastic member 67 is constant. That is, as shown in FIG. 5A, the pressing force P l of the elastic member 67 is increased relative to the increase in the crush amount x of the elastic member 67. The value obtained by multiplying the pressing force P l of the elastic member 67 in the axial direction of the movement amount δl of the sheath assembly 54 relative to the coupling tube 71, corresponding to a value obtained by multiplying the rotation operation force amount P theta in rotation angle δθ of the cam mechanism It will be. That is, P l (x) * δl∝P θ * δθ. Here, when the pressure angle α of the operating surface 76 of the cam surface 74 is constant with respect to the rotation angle θ of the cam mechanism, the axial movement amount δl of the sheath assembly 54 with respect to the rotation angle amount δθ of the cam mechanism, That is, δl / δθ is constant. In this case, as the rotation angle θ of the cam mechanism increases, the amount x of collapse of the elastic member 67 increases, and as the pressing force amount P l (x) increases, the necessary rotational operation force amount P θ ∝P l (x ) * (Δl / δθ) will be increased. On the other hand, in this embodiment, as shown in FIG. 5B, the pressure angle α of the operating surface 76 of the cam surface 74 is appropriately increased with respect to the increase of the rotation angle θ of the cam mechanism, and the rotation angle of the cam mechanism By appropriately reducing the axial movement amount δl of the sheath assembly 54 with respect to the amount δθ, that is, δl / δθ, the rotational operation force amount P θ ∝P l (x) * (δl / δθ) is made constant.

カム機構では、カムピン69が係合される連結位置としての4つの係合凹面80が周方向に等間隔で配置されており、シースユニット22はハンドピース21に対して4つの相対的回転配置で連結可能である。シースユニット22の基端部をハンドピース21の先端部に軸方向に内挿する際に、カムピン69を挿入する導入溝部82を4つの導入溝部82の内から選択することにより、ハンドピース21に対するシースユニット22の相対的回転配置を4つの相対的回転配置の内から選択することが可能である。さらに、ハンドピース21にシースユニット22が連結されている場合に、ハンドピース21に対してシースユニット22を連結方向へと回転操作することにより、カムピン69が係合凹面80から回転凸面79を乗り越えて移動される。弾性部材67の作用により、カムピン69は先端向きに押圧されているため、カムピン69は、それまで押圧されていたカム面74から離脱されて先端向きに移動され、当該カム受部73の連結方向側に隣り合うカム受部73のカム面74へと移行される。ハンドピース21に対してシースユニット22をさらに連結方向へと回転操作することにより、カムピン69は移行されたカム面74に沿って移動されて再び係合凹面80に係合されて、ハンドピース21にシースユニット22が連結される。このように、ハンドピース21にシースユニット22が連結されている場合に、ハンドピース21に対してシースユニット22を連結方向へと回転操作することにより、ハンドピース21に対してシースユニット22を4つの相対的回転配置間で移動させることが可能である。従って、ハンドピース21のハンドスイッチ部49に対して、プローブ61の処置部62を任意の方向に配置することが可能となる。   In the cam mechanism, four engagement concave surfaces 80 as connection positions with which the cam pins 69 are engaged are arranged at equal intervals in the circumferential direction, and the sheath unit 22 is arranged in four relative rotational arrangements with respect to the handpiece 21. Can be linked. When the proximal end portion of the sheath unit 22 is inserted into the distal end portion of the handpiece 21 in the axial direction, the introduction groove portion 82 into which the cam pin 69 is inserted is selected from the four introduction groove portions 82, thereby The relative rotational arrangement of the sheath unit 22 can be selected from among four relative rotational arrangements. Further, when the sheath unit 22 is connected to the handpiece 21, the cam pin 69 gets over the rotating convex surface 79 from the engaging concave surface 80 by rotating the sheath unit 22 in the connecting direction with respect to the handpiece 21. Moved. Since the cam pin 69 is pressed toward the distal end by the action of the elastic member 67, the cam pin 69 is detached from the cam surface 74 that has been pressed so far and moved toward the distal end, and the connecting direction of the cam receiving portion 73. Transition is made to the cam surface 74 of the cam receiving portion 73 adjacent to the side. When the sheath unit 22 is further rotated in the connecting direction with respect to the handpiece 21, the cam pin 69 is moved along the shifted cam surface 74 and is again engaged with the engaging concave surface 80. The sheath unit 22 is coupled to the above. As described above, when the sheath unit 22 is coupled to the handpiece 21, the sheath unit 22 is rotated with respect to the handpiece 21 by rotating the sheath unit 22 in the coupling direction with respect to the handpiece 21. It is possible to move between two relative rotational arrangements. Therefore, the treatment portion 62 of the probe 61 can be arranged in an arbitrary direction with respect to the hand switch portion 49 of the handpiece 21.

従って、本実施形態の外科処置具は、以下の効果を奏する。   Accordingly, the surgical instrument according to this embodiment has the following effects.

本実施形態の外科処置具では、ハンドピース21とシースユニット22との連結に際して、弾性部材67の変形量を一定に調整することで、弾性部材67からプローブ61に付与される弾性力を一定に調整し、ホーン31とプローブ61との間に作用する押圧力量を一定に調整している。特に、ハンドピース21とシースユニット22との連結にカム機構を用いることにより、押圧力量を非常に正確に調整することが可能となっている。ここで、押圧力量が適切な範囲よりも小さい場合には、ホーン31からプローブ61へと超音波振動を正常に伝達することができなくなる。一方、押圧力量が適切な範囲よりも大きい場合には、力学的インピーダンスが高くなり、振動子24の抵抗が大きくなって、振動効率が低下する。また、弾性部材67の押圧力量に抗してハンドピース21に対してシースユニット22を回転操作するのに必要な回転操作力量が大きくなって、回転操作が困難となる。本実施形態では、押圧力量が適切な範囲内に調整されるため、ホーン31及びプローブ61を適切に超音波振動させることが可能となっており、また、回転操作が容易となっている。   In the surgical instrument of the present embodiment, when the handpiece 21 and the sheath unit 22 are connected, the elastic force applied from the elastic member 67 to the probe 61 is made constant by adjusting the deformation amount of the elastic member 67 to be constant. The amount of pressing force acting between the horn 31 and the probe 61 is adjusted to be constant. In particular, by using a cam mechanism for connecting the handpiece 21 and the sheath unit 22, the amount of pressing force can be adjusted very accurately. Here, when the amount of pressing force is smaller than the appropriate range, ultrasonic vibration cannot be normally transmitted from the horn 31 to the probe 61. On the other hand, when the amount of pressing force is larger than the appropriate range, the mechanical impedance increases, the resistance of the vibrator 24 increases, and the vibration efficiency decreases. Further, the amount of rotational operation force required to rotate the sheath unit 22 with respect to the handpiece 21 against the amount of pressing force of the elastic member 67 becomes large, and the rotation operation becomes difficult. In this embodiment, since the amount of pressing force is adjusted within an appropriate range, the horn 31 and the probe 61 can be appropriately ultrasonically vibrated, and the rotation operation is facilitated.

また、カム機構において回転角度に対して圧力角を変化させることにより、ハンドピース21及びシースユニット22への回転操作において、弾性部材67の変形量にかかわらず回転操作力量が一定となるようにしている。このため、回転操作を円滑に行うことが可能となっている。   Further, by changing the pressure angle with respect to the rotation angle in the cam mechanism, in the rotation operation to the handpiece 21 and the sheath unit 22, the rotation operation force is made constant regardless of the deformation amount of the elastic member 67. Yes. For this reason, it is possible to perform a rotation operation smoothly.

さらに、カムピン69が連結凸面78を越えて係合凹面80に係合されるようになっており、係合凹面80への係合の際にクリック感が生じるため、ハンドピース21にシースユニット22が連結されたことを認識することが可能となっている。   Further, since the cam pin 69 is engaged with the engaging concave surface 80 beyond the connecting convex surface 78 and a click feeling is generated when the cam pin 69 is engaged with the engaging concave surface 80, the sheath unit 22 is attached to the handpiece 21. Can be recognized.

加えて、周方向について互いに異なる位置に配置されている4つの係合凹面80の内の所望の係合凹面80にカムピン69を係合することができ、4つの相対的回転配置の内の所望の相対的回転配置でハンドピース21にシースユニット22を連結することが可能となっている。このため、外科用処置具を当座の処置に適した形態とすることが可能となっている。特に、ハンドピース21の保持の仕方はハンドピース21におけるハンドスイッチ部49の配置に応じて適宜定まり、本実施形態のようにプローブ61の処置部62が非回転対称形状を有する場合には、ハンドピース21に対してシースユニット22が回転不能で処置部62の向きが変更できないと外科処置具が使いにくくなるが、本実施形態ではかかかる事態が防止されている。   In addition, the cam pin 69 can be engaged with a desired engagement concave surface 80 among the four engagement concave surfaces 80 that are arranged at positions different from each other in the circumferential direction. It is possible to connect the sheath unit 22 to the handpiece 21 with the relative rotational arrangement. For this reason, it is possible to make the surgical treatment instrument into a form suitable for the current treatment. In particular, the way of holding the handpiece 21 is appropriately determined according to the arrangement of the hand switch 49 in the handpiece 21, and when the treatment section 62 of the probe 61 has a non-rotation symmetric shape as in the present embodiment, If the sheath unit 22 cannot rotate with respect to the piece 21 and the orientation of the treatment portion 62 cannot be changed, the surgical instrument becomes difficult to use, but this situation is prevented in this embodiment.

さらにまた、プローブ61において太外径部66よりも細径のテーパ部64及び細外径部63を形成し、テーパ部64にフランジ状の押圧部65を形成することで、押圧部65の外径を太外径部66の外径以下としている。即ち、シースユニット22が太径化することが回避されており、外科処置具の操作性の低下が防止されている。特に、本実施形態のような、比較的短尺の開腹手術用の外科処置具では、外科処置具の太径化により、外科処置具の先端部の処置部62が視認しにくくなり、外科処置具の操作性が低下することとなるが、本実施形態ではかかる事態が防止されている。   Furthermore, the probe 61 is formed with a taper portion 64 and a thin outer diameter portion 63 that are thinner than the thick outer diameter portion 66, and a flange-like pressing portion 65 is formed on the taper portion 64. The diameter is equal to or smaller than the outer diameter of the thick outer diameter portion 66. That is, the diameter of the sheath unit 22 is avoided and the operability of the surgical instrument is prevented from being lowered. In particular, in a surgical instrument for relatively short laparotomy as in the present embodiment, due to the increase in diameter of the surgical instrument, it becomes difficult to visually recognize the treatment part 62 at the distal end of the surgical instrument. However, in this embodiment, such a situation is prevented.

なお、本実施形態では、非回転対称形状を有する処置部を用いているが、本発明は、例えばプローブの先端部が球状をなすような、回転対称形状を有する処置部にも適用可能である。   In this embodiment, the treatment portion having a non-rotationally symmetric shape is used. However, the present invention can also be applied to a treatment portion having a rotationally symmetric shape, for example, the tip of the probe is spherical. .

また、本発明は、上述した開腹手術用の超音波出力併用型高周波処置具以外の様々な外科処置装置にも適用可能である。   The present invention can also be applied to various surgical treatment apparatuses other than the above-described ultrasonic output combined high-frequency treatment instrument for laparotomy.

例えば、本発明は、図6に示されるような、内視鏡手術用の超音波出力併用型高周波処置具にも適用可能である。図6に示される外科処置具では、上述した実施形態と同様な構成のハンドピース21、シースユニット22が用いられている。但し、シースユニット22は長尺であり、先端側シース55の先端部には挿入シース86の基端部が内挿固定されており、挿入シース86にはプローブ61が挿通されている。プローブ61の軸方向長さは超音波振動の1/2波長の整数倍の長さとなっている。   For example, the present invention is also applicable to an ultrasonic output combined high-frequency treatment instrument for endoscopic surgery as shown in FIG. In the surgical instrument shown in FIG. 6, the handpiece 21 and the sheath unit 22 having the same configuration as those of the above-described embodiment are used. However, the sheath unit 22 is long, and the proximal end portion of the insertion sheath 86 is inserted and fixed at the distal end portion of the distal end side sheath 55, and the probe 61 is inserted through the insertion sheath 86. The axial length of the probe 61 is an integral multiple of 1/2 wavelength of ultrasonic vibration.

また、例えば、本発明は、図7に示されるような、内視鏡手術用の超音波処置具にも適用可能である。図7に示される外科処置具では、シースユニット22の挿入シース86にプローブ61が挿通されている。挿入シース86の先端部にはジョー92が枢着されており、ジョー92はプローブ61の先端部の処置部62に対して開閉されてプローブ61と共同して生体組織を把持可能である。シースユニット22の基端部はハンドルユニット88の先端側に連結されている。ハンドルユニット88の円筒状の本体部89には一対のハンドル91が突設されており、一対のハンドル91を開閉操作することによりジョー92が開閉作動される。また、先端側のハンドル91には、ハンドスイッチ部49が配設されている。ハンドルユニット88の本体部89の基端側には、振動子ユニット87の先端部が着脱自在に連結されている。ここで、振動子ユニット87は、上述した実施形態のハンドピース21と同様な構成を有する。但し、本変形例では、ハンドスイッチ部49は振動子ユニット87ではなくハンドルユニット88に配設されており、ハンドルユニット88と振動子ユニット87とは適切な電気的接続機構により接続され、ハンドスイッチ部49が装置本体に接続される。また、振動子ユニット87の先端部には上述した実施形態と同様なカムピンが配設されており、ハンドルユニット88の本体部89内にはカム枠が配設されている。そして、カム機構によりハンドルユニット88に振動子ユニット87を連結することにより、ハンドルユニット88の本体部89内で、プローブ61の基端部とホーン31の先端部とが互いに押圧され、連結されるようになっている。   Further, for example, the present invention can be applied to an ultrasonic treatment instrument for endoscopic surgery as shown in FIG. In the surgical instrument shown in FIG. 7, the probe 61 is inserted through the insertion sheath 86 of the sheath unit 22. A jaw 92 is pivotally attached to the distal end portion of the insertion sheath 86, and the jaw 92 can be opened and closed with respect to the treatment portion 62 at the distal end portion of the probe 61, and can grasp a living tissue in cooperation with the probe 61. The proximal end portion of the sheath unit 22 is connected to the distal end side of the handle unit 88. A pair of handles 91 project from the cylindrical main body 89 of the handle unit 88, and the jaw 92 is opened and closed by opening and closing the pair of handles 91. A hand switch 49 is disposed on the handle 91 on the distal end side. The distal end portion of the vibrator unit 87 is detachably connected to the proximal end side of the main body portion 89 of the handle unit 88. Here, the vibrator unit 87 has the same configuration as the handpiece 21 of the above-described embodiment. However, in this modified example, the hand switch unit 49 is disposed not in the vibrator unit 87 but in the handle unit 88, and the handle unit 88 and the vibrator unit 87 are connected by an appropriate electrical connection mechanism. The unit 49 is connected to the apparatus main body. In addition, a cam pin similar to that of the above-described embodiment is disposed at the distal end portion of the vibrator unit 87, and a cam frame is disposed in the main body portion 89 of the handle unit 88. Then, by connecting the vibrator unit 87 to the handle unit 88 by the cam mechanism, the proximal end portion of the probe 61 and the distal end portion of the horn 31 are pressed and connected to each other within the main body portion 89 of the handle unit 88. It is like that.

21…第1のユニット(ハンドピース)、22…第2のユニット(シースユニット)、31…第1の振動伝達部材(ホーン)、39…第1の保持部材(内側ハウジング)、54…第2の保持部材(シース組体)、61…第2の振動伝達部材(プローブ)、63…細外径部、64…テーパ部、65…押圧部、66…太外径部、67…弾性部材、69,74…調整連結機構(カム機構)、69…作動部(カムピン)、74…作動受部(カム面)、78…告知機構(凹凸形状、連結凸面)、80…連結位置(係合凹面)。   21 ... 1st unit (handpiece), 22 ... 2nd unit (sheath unit), 31 ... 1st vibration transmission member (horn), 39 ... 1st holding member (inner housing), 54 ... 2nd Holding member (sheath assembly), 61 ... second vibration transmission member (probe), 63 ... narrow outer diameter part, 64 ... taper part, 65 ... pressing part, 66 ... thick outer diameter part, 67 ... elastic member, 69, 74 ... adjustment coupling mechanism (cam mechanism), 69 ... operation part (cam pin), 74 ... operation receiving part (cam surface), 78 ... notification mechanism (concave / convex shape, connection convex surface), 80 ... connection position (engagement concave surface) ).

Claims (9)

軸方向に延び端部を有し超音波振動を伝達する第1の振動伝達部材、及び、前記第1の振動伝達部材を保持している第1の保持部材、を有する第1のユニットと、
軸方向に延び端部を有し超音波振動を伝達する第2の振動伝達部材、前記第2の振動伝達部材の軸方向に移動可能に前記第2の振動伝達部材を保持している第2の保持部材、及び、前記第2の振動伝達部材と前記第2の保持部材との間に設けられ、前記第2の振動伝達部材の軸方向についての前記第2の振動伝達部材と前記第2の保持部材との相対的配置に応じて変形され、前記第2の振動伝達部材に前記第2の振動伝達部材の軸方向への弾性力を付与する弾性部材、を有する第2のユニットと、
前記第1のユニットと前記第2のユニットとを互いに連結し、前記第1の振動伝達部材と前記第2の振動伝達部材とを共軸に配置して前記第1の振動伝達部材の端部と前記第2の振動伝達部材の端部とを互いに当接させると共に、共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的配置を一定に調整することにより前記弾性部材の変形量を一定に調整する調整連結機構と、
を具備することを特徴とする外科処置装置。
A first unit having a first vibration transmission member that extends in the axial direction and transmits ultrasonic vibrations, and a first holding member that holds the first vibration transmission member;
A second vibration transmission member having an end portion extending in the axial direction and transmitting ultrasonic vibrations, and a second vibration transmission member holding the second vibration transmission member movably in the axial direction of the second vibration transmission member. Holding member, and between the second vibration transmitting member and the second holding member, the second vibration transmitting member and the second in the axial direction of the second vibration transmitting member. A second unit having an elastic member that is deformed according to a relative arrangement with the holding member, and applies an elastic force in an axial direction of the second vibration transmission member to the second vibration transmission member;
The first unit and the second unit are connected to each other, and the first vibration transmission member and the second vibration transmission member are arranged coaxially and an end portion of the first vibration transmission member And the end portion of the second vibration transmitting member are brought into contact with each other, and the relative arrangement of the first holding member and the second holding member in the coaxial direction is adjusted to be constant. An adjustment coupling mechanism for adjusting the amount of deformation of the elastic member to a constant;
A surgical treatment apparatus comprising:
前記調整連結機構は、カム機構を有し、
前記カム機構は、前記第1の保持部材と前記第2の保持部材との内の一方の保持部材に設けられている作動部と、前記第1の保持部材と前記第2の保持部材との内の他方の保持部材に設けられ軸を中心として螺旋状に延びている作動受部と、を有し、前記作動部は前記作動受部に沿って移動され、前記作動部が前記作動受部の連結位置に配置された場合に前記第1のユニットと前記第2のユニットとが互いに連結される、
ことを特徴とする請求項1に記載の外科処置装置。
The adjustment coupling mechanism has a cam mechanism,
The cam mechanism includes an operating portion provided in one holding member of the first holding member and the second holding member, and the first holding member and the second holding member. An operation receiving portion that is provided on the other holding member and extends in a spiral shape about an axis, and the operation portion is moved along the operation reception portion, and the operation portion is the operation reception portion. The first unit and the second unit are connected to each other when arranged at the connection position of
The surgical treatment apparatus according to claim 1.
前記調整連結機構は、前記弾性部材の弾性力に抗して共軸方向に前記第1の保持部材と前記第2の保持部材とを相対的に移動させるための操作について、必要な操作力量が一定となるように、操作量に対する共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的移動量を、共軸方向についての前記第1の保持部材と前記第2の保持部材との相対的配置に応じて変化させている、
ことを特徴とする請求項1に記載の外科処置装置。
The adjustment coupling mechanism has a necessary amount of operation force for an operation for relatively moving the first holding member and the second holding member in the coaxial direction against the elastic force of the elastic member. The relative movement amount of the first holding member and the second holding member in the coaxial direction with respect to the operation amount is set to be constant, and the first holding member and the second holding amount in the coaxial direction are set. It is changed according to the relative arrangement with the holding member of
The surgical treatment apparatus according to claim 1.
前記カム機構は、前記弾性部材の弾性力に抗して共軸方向に前記第1の保持部材と前記第2の保持部材とを相対的に移動させるための回転操作について、回転操作力量が一定となるように、回転角度に対して圧力角を変化させている、
ことを特徴とする請求項2に記載の外科処置装置。
The cam mechanism has a constant rotational operation force amount with respect to a rotational operation for moving the first holding member and the second holding member relative to each other in the coaxial direction against the elastic force of the elastic member. The pressure angle is changed with respect to the rotation angle so that
The surgical treatment apparatus according to claim 2.
前記調整連結機構は、前記第1のユニットと前記第2のユニットとが連結されたことを告知する告知機構を有する、
ことを特徴とする請求項1に記載の外科処置装置。
The adjustment coupling mechanism has a notification mechanism for notifying that the first unit and the second unit are coupled.
The surgical treatment apparatus according to claim 1.
前記カム機構は、前記作動受部において連結位置の手前で前記作動受部に交差する方向に突没している凹凸形状を有する、
ことを特徴とする請求項2に記載の外科処置装置。
The cam mechanism has a concavo-convex shape projecting and sinking in a direction intersecting the operation receiving portion before the connection position in the operation receiving portion.
The surgical treatment apparatus according to claim 2.
前記調整連結機構は、前記第1のユニットと前記第2のユニットとを共軸を中心とする複数の相対的回転配置で連結可能である、
ことを特徴とする請求項1に記載の外科処置装置。
The adjustment coupling mechanism is capable of coupling the first unit and the second unit with a plurality of relative rotational arrangements around a coaxial axis.
The surgical treatment apparatus according to claim 1.
前記カム機構は、周方向について互いに異なる位置に配置されている第1及び第2の連結位置を有する、
ことを特徴とする請求項2に記載の外科処置装置。
The cam mechanism has first and second coupling positions arranged at different positions in the circumferential direction.
The surgical treatment apparatus according to claim 2.
前記第2の振動伝達部材は、前記第2の振動伝達部材において軸方向の一端側に形成されている太外径部と、前記第2の振動伝達部材において軸方向の他端側に形成され前記太外径部よりも外径の小さな細外径部と、前記第2の振動伝達部材において前記太外径部と前記細外径部との間に形成され軸方向の一端側から他端側へと外径の減少するテーパ部と、前記テーパ部あるいは前記細外径部に設けられ径方向に突出している押圧部と、を有し、
前記弾性部材は、軸方向について前記押圧部と前記第2の保持部材との間に設けられている、
ことを特徴とする請求項1に記載の外科処置装置。
The second vibration transmission member is formed on a thick outer diameter portion formed on one end side in the axial direction of the second vibration transmission member, and on the other end side in the axial direction of the second vibration transmission member. A thin outer diameter portion having an outer diameter smaller than that of the thick outer diameter portion, and the second vibration transmitting member formed between the thick outer diameter portion and the thin outer diameter portion, from one end side in the axial direction to the other end. A taper portion with an outer diameter decreasing toward the side, and a pressing portion provided in the taper portion or the thin outer diameter portion and projecting in the radial direction,
The elastic member is provided between the pressing portion and the second holding member in the axial direction.
The surgical treatment apparatus according to claim 1.
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